Gene/Event |
Cancer Type |
Patient |
Variant |
Mutation Level |
FAM169A |
Colorectal Cancer | p004_CRC_A01 |
Chr5:74134927:G>A |
Branch mutation |
FAM169A |
Esophageal Squamous Cell Carcinoma | p139_EC0949 |
p.S12R |
Private mutation |
FAM169A |
Esophageal Squamous Cell Carcinoma | p139_EC0949 |
p.S12N |
Private mutation |
FAM169A |
Gastric Adenocarcinoma | p011_MSI-H1 |
p.P490T |
Private mutation |
FAM169A |
Gastric Carcinoma | p106_GC07 |
p.K146T |
Private mutation |
FAM169A |
Medulloblastoma | p072_MB6 |
Chr5:74226440:A>C |
Branch mutation |
FAM169A |
Medulloblastoma | p072_MB6 |
Chr5:74226441:A>G |
Branch mutation |
FAM169A |
Clear Cell Renal Cell Carcinoma | p019_RK26 |
Chr5:74078809:p.V>F |
Branch mutation |
FAM169A |
Renal Cell Carcinoma | p073_RCC7 |
Chr5:74078809:C>A |
Branch mutation |